Sensitive Absorption Imaging of Single Atoms in Front of a Mirror

In this paper we show that the sensitivity of absorption imaging of ultracold atoms can be significantly improved by imaging in a standing-wave configuration. We present simulations of single-atom absorption imaging both for a travelling-wave and a standing-wave imaging setup, based on a scattering approach to calculate the optical density of a single atom. We find that the optical density of a single atom is determined only by the numerical aperture of the imaging system. We determine optimum imaging parameters, taking all relevant sources of noise into account. For reflective imaging we find an improvement of 1.7 in the maximum signal-to-noise ratio can be achieved. This is particularly useful for imaging in the vicinity of an atom chip, where a reflective surface is naturally present.

High-Precision Measurement of Rydberg State Hyperfine Splitting in a Room-Temperature Vapour Cell

We present direct measurements of the hyperfine splitting of Rydberg states in rubidium 87 using Electromagnetically Induced Transparency (EIT) spectroscopy in a room-temperature vapour cell. With this method, and in spite of Doppler-broadening, line-widths of 3.7 MHz FWHM, i.e. significantly below the intermediate state natural linewidth are reached. This allows resolving hyperfine splittings for Rydberg s-states with n=20...24. With this method we are able to determine Rydberg state hyperfine splittings with an accuracy of approximately 100 kHz. Ultimately our method allows accuracies of order 5 kHz to be reached. Furthermore we present a direct measurement of hyperfine-resolved Rydberg state Stark-shifts. These results will be of great value for future experiments relying on excellent knowledge of Rydberg-state energies and

Spatially Resolved Excitation of Rydberg Atoms and Surface Effects on an Atom Chip

We demonstrate spatially resolved, coherent excitation of Rydberg atoms on an atom chip. Electromagnetically induced transparency (EIT) is used to investigate the properties of the Rydberg atoms near the gold coated chip surface. We measure distance dependent shifts (~10 MHz) of the Rydberg energy levels caused by a spatially inhomogeneous electric field. The measured field strength and distance dependence is in agreement with a simple model for the electric field produced by a localized patch of Rb adsorbates deposited on the chip surface during experiments. The EIT resonances remain narrow (< 4 MHz) and the observed widths are independent of atom-surface distance down to ~20 mum, indicating relatively long lifetime of the Rydberg states. Our results open the way to studies of dipolar physics, collective excitations, quantum metrology and quantum information processing involving interacting Rydberg excited atoms on atom chips.

Observation of Stueckelberg oscillations in dipole-dipole interactions

We have observed Stueckelberg oscillations in the dipole-dipole interaction between Rydberg atoms with an externally applied radio-frequency field. The oscillating RF field brings the interaction between cold Rydberg atoms in two separated volumes into resonance. We observe multi-photon transitions when varying the amplitude of the RF-field and the static electric field offset. The angular momentum states we use show a quadratic Stark shift, which leads to a fundamentally different behavior than linearly shifting states. Both cases are studied theoretically using the Floquet approach and are compared. The amplitude of the sidebands, related to the interaction strength, is given by the Bessel function in the linearly shifting case and by the generalized Bessel function in the quadratically shifting case. The oscillatory behavior of both functions corresponds to Stueckelberg oscillations, an interference effect described by the semi-classical Landau-Zener-Stueckelberg model. The measurements prove coherent dipole-dipole interaction during at least 0.6 micro-seconds.

Radio-frequency driven dipole-dipole interactions in spatially separated volumes

Radio-frequency (rf) fields in the MHz range are used to induce resonant energy transfer between cold Rydberg atoms in spatially separated volumes. After laser preparation of the Rydberg atoms, dipole-dipole coupling excites the 49s atoms in one cylinder to the 49p state while the 41d atoms in the second cylinder are transferred down to the 42p state. The energy exchanged between the atoms in this process is 33 GHz. An external rf-field brings this energy transfer into resonance. The strength of the interaction has been investigated as a function of amplitude (0-1 V/cm) and frequency (1-30 MHz) of the rf-field and as a function of a static field offset. Multi-photon transitions up to fifth order as well as selection rules prohibiting the process at certain fields have been observed. The width of the resonances has been reduced compared to earlier results by switching off external magnetic fields of the magneto-optical trap, making sub-MHz spectroscopy possible. All features are well reproduced by theoretical calculations taking the strong ac-Stark shift due to the rf-field into account.